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Understanding ISO 13485 Medical Device QMS Training

Posted by : team training | Aug 29, 2012
Come & Join us for the training.

Call us now as it is limited seat.


Course Objectives
This course will help you to understand the best way of integrating risk management into your organization and give you the tools and techniques necessary to ensure the risk management process effectively meets your requirements and the requirements of international regulators.


For Whom
Various professional groups, including:
o Regulatory affairs professionals
o Quality assurance professionals responsible for design and/or manufacturing
o Design engineering and market managers responsible for medical devices within market processes
o Clinical and product management teams.

Register here - www

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